Sarah Scollon
- Genetics top 5%
- Pediatrics, Perinatology and Child Health top 5%
- Molecular Biology
- Public Health, Environmental and Occupational Health top 10%
- Neurology top 10%
- Co-authors
- Kami Wolfe SchneiderBarbara A. BernhardtSharon E. PlonMyra I. RocheDenise PerryDebra SkinnerAshley N. TomlinsonLaura M. Amendola
- Topics
- Genomics and Rare Diseases (17 papers)BRCA gene mutations in cancer (17 papers)Childhood Cancer Survivors' Quality of Life (8 papers)
- Partner nations
- United StatesCanadaAustralia
In The Last Decade
Sarah Scollon
43 papers receiving 977 citations
Peers
Comparison fields: 5 of 78
- Genetics 473
- Pediatrics, Perinatology and Child Health 267
- Molecular Biology 199
- Public Health, Environmental and Occupational Health 193
- Neurology 178
Countries citing papers authored by Sarah Scollon
This map shows the geographic impact of Sarah Scollon's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sarah Scollon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah Scollon more than expected).
Fields of papers citing papers by Sarah Scollon
This network shows the impact of papers produced by Sarah Scollon. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sarah Scollon. The network helps show where Sarah Scollon may publish in the future.
Co-authorship network of co-authors of Sarah Scollon
This figure shows the co-authorship network connecting the top 25 collaborators of Sarah Scollon. A scholar is included among the top collaborators of Sarah Scollon based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sarah Scollon. Sarah Scollon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 3 | |
| 3 | 6 | |
| 4 | 9 | |
| 5 | 0 | |
| 6 | 0 | |
| 7 | 1 | |
| 8 | 5 | |
| 9 | 4 | |
| 10 | 2 | |
| 11 | 10 | |
| 12 | 0 | |
| 13 | 6 | |
| 14 | 6 | |
| 15 | 16 | |
| 16 | 16 | |
| 17 | 17 | |
| 18 | 17 | |
| 19 | 4 | |
| 20 | 1 |
About Sarah Scollon
Sarah Scollon is a scholar working on Genetics, Cancer Research and Pediatrics, Perinatology and Child Health, having authored 47 papers that have together received 991 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (17 papers), BRCA gene mutations in cancer (17 papers) and Childhood Cancer Survivors' Quality of Life (8 papers). The work is most often cited by research in Genetics (473 citations), Pediatrics, Perinatology and Child Health (267 citations) and Neurology (178 citations). Sarah Scollon has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Kami Wolfe Schneider, Barbara A. Bernhardt, Sharon E. Plon, Myra I. Roche, Denise Perry, Debra Skinner, Ashley N. Tomlinson, Laura M. Amendola, Harriet Druker and Wendy Kohlmann. Their work appears in journals such as Journal of Clinical Oncology, Cancer and Cancer Research.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.